[Federal Register Volume 75, Number 218 (Friday, November 12, 2010)]
[Notices]
[Page 69467]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-28522]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated June 17, 2010, and published in the Federal 
Register on June 28, 2010, (75 FR 36683), Wildlife Laboratories, Inc., 
1401 Duff Drive, Suite 400, Fort Collins, Colorado 80524, made 
application by renewal to the Drug Enforcement Administration (DEA) to 
be registered as a bulk manufacturer of Carfentanil (9743), a basic 
class of controlled substance listed in schedule II.
    The company will manufacture the above listed controlled substance 
for sale to veterinary pharmacies, zoos, and for other animal and 
wildlife applications.
    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. 823(a) and determined that the registration of 
Wildlife Laboratories, Inc. to manufacture the listed basic class of 
controlled substance is consistent with the public interest at this 
time. DEA has investigated Wildlife Laboratories, Inc. to ensure that 
the company's registration is consistent with the public interest. The 
investigation has included inspection and testing of the company's 
physical security systems, verification of the company's compliance 
with state and local laws, and a review of the company's background and 
history. Therefore, pursuant to 21 U.S.C. 823(a), and in accordance 
with 21 CFR 1301.33, the above named company is granted registration as 
a bulk manufacturer of the basic class of controlled substance listed.

    Dated: November 1, 2010.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2010-28522 Filed 11-10-10; 8:45 am]
BILLING CODE 4410-09-P